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Shoulder Impingement Syndrome clinical trials

View clinical trials related to Shoulder Impingement Syndrome.

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NCT ID: NCT04794933 Completed - Clinical trials for Subacromial Impingement Syndrome

PNF in Subacromial Impingement Syndrome

Start date: December 2013
Phase: N/A
Study type: Interventional

Although proprioceptive neuromuscular facilitation (PNF) techniques have been used in the treatment of different shoulder problems, PNF techniques in scapular and upper trunk patterns with extremity pattern have not been considered as a possible option for the treatment of Subacromial Impingement Syndrome (SIS). The aim of this study was to evaluate the effects of different PNF patterns in SIS.

NCT ID: NCT04784377 Completed - Clinical trials for Subacromial Impingement Syndrome

High and Low Laser for Subacromial Impingement Syndrome

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

Shoulder pain is the third most common musculoskeletal problem after lumbar and neck diseases in clinical practice, and the most common cause of shoulder pain is subacromial impingement syndrome. The main goal of treatment is to reduce pain and to solve the mechanical problem that causes functional impairment. Low-level laser treatment is an increasingly used treatment modality in the treatment of subacromial impingement syndrome as in many musculoskeletal diseases, as it promotes cell proliferation and tissue regeneration by its anti-inflammatory and photobiostimulation properties. Also, High-intensity laser therapy is a treatment method that is gaining popularity in the recent years. These ultra-short impulses effect a deep action in the biological tissue (3-4 cm), with a homogeneous distribution of the light source in the irradiated soft tissue, but without excessive thermal enhancements. It reduces pain and edema with photomechanic effects in deep tissues. As far as the investigators know, there are no studies comparing these two treatment modalities in subacromial impingement syndrome yet. This study was planned to compare the efficacy of High-intensity laser therapy and low-intensity laser therapy in treatment of patients with subacromial impingement syndrome.

NCT ID: NCT04779190 Completed - Clinical trials for Subacromial Impingement Syndrome

Physical Therapy in Shoulder Impingement Syndrome

Start date: March 4, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effects of low-level laser therapy (LLLT) and therapeutic ultrasound combined with home-based exercise in comparison with home-based exercise alone in patients with subacromial impingement syndrome (SIS). Participants are going to evaluate before training, and at the 1-month follow-up and 3-month follow-up using the visual analog scale (VAS) scores for pain during activity, at rest, and at night, and the Shoulder Pain and Disability Index (SPADI).

NCT ID: NCT04766905 Completed - Clinical trials for Shoulder Impingement Syndrome

Mini Lateral Shoulder Approach

MLSA
Start date: January 17, 2019
Phase: N/A
Study type: Interventional

The incision is very useful and easy for the direct lateral shoulder joint exposure.

NCT ID: NCT04759027 Completed - Rotator Cuff Tears Clinical Trials

Reliability of the Subacromial Distance Measurements With Standard Radiographic Imaging

Start date: May 1, 2021
Phase:
Study type: Observational

Patients with complaints of shoulder pain or limitation of motion, who admitted to outpatient orthopaedic clinic will be analyzed. It was planned to measure the subacromial distance using standardized both shoulder ap, true ap and outlet radiographs, and ultrasound to be performed for shoulder circumference soft tissue and muscle-tendon evaluation. The measurement made by the physical therapy and rehabilitation specialist with ultrasound will be considered to be accurate, and it was planned to evaluate the reliability of the graphy measurements by comparing this measurement with the measurements in the graphs. In addition, it was planned to evaluate the intra-observer and inter-observer compliance by re-measuring the subacromial distance on the radiograph by orthopedic doctors of three different seniority levels with an interval of one month.

NCT ID: NCT04701814 Completed - Clinical trials for Shoulder Impingement Syndrome

The Effect of Biomechanical Scapular Mobilization With Movement and Motor Learning

BSMWM
Start date: May 5, 2021
Phase: N/A
Study type: Interventional

the study about new mobilization technique used in shoulder impingement syndrome patient to increase the range of motion of elevation, decrease the pain, and increasing the function level, this technique is based on normal mechanics that occur inside the joint during certain movement.

NCT ID: NCT04692649 Completed - Shoulder Pain Clinical Trials

Comparison of Pragmatic Posterior Capsular Stretch and Crossbody Stretch on the Shoulder Mobility

Start date: January 5, 2021
Phase: N/A
Study type: Interventional

Various stretches are used to lengthen the posterior shoulder capsule. No study has reported the comparison of the pragmatic posterior capsular stretch and cross body stertch

NCT ID: NCT04676919 Completed - Clinical trials for Subacromial Impingement Syndrome

The Effect of Phonophoresis in Subacromial Impingement Syndrome.

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Subacromial impingement syndrome (SIS) is a dysfunction caused by an impingement of the rotator cuff tendon between the head of the humerus and the acromion as a result of changes in the subacromial space. The patients' symptoms, such as pain, limited joint mobility and reduced strength, may lead to a diagnosis of SIS. The conservative treatment of individuals with SIS is includes analgesics and non-steroidal anti-inflammatory drugs (NSAIDs), steroid injections and physiotherapy. Ultrasound therapy is one of the common physiotherapy applications for SIS, but its effectiveness is controversial. Phonophoresis is a combination of ultrasound therapy and medical therapy. In phonophoresis, a medicine in gel form is used as a transmitter with ultrasound instead of the aquatic conductor gel. It was hypothesized that ultrasound waves favoring the penetration of an anti-inflammatory drug would lead to an improved response to the treatment of SIS. However, the effectiveness of ultrasound modes (pulsed or continuous) can be used in phonophoresis is debatable. The purpose of this study is to determine the effect of ultrasound therapy, pulsed mode ultrasound and continuous mode ultrasound phonophoresis in patients with SIS.

NCT ID: NCT04667273 Completed - Clinical trials for Subacromial Impingement Syndrome

Effectiveness of Neuromuscular Electrical Stimulation in Patients With Subacromial Impingement Syndrome

Start date: December 20, 2020
Phase: N/A
Study type: Interventional

Subacromial Impingement Syndrome (SIS) is one of the musculoskeletal system problems. SIS, which is the most common cause of shoulder pain, constitutes 44-65% of complaints of shoulder pain. Studies have shown that exercise is effective in treating patients with SIS, but the effectiveness and superiority of Neuromuscular Electrical Stimulation (NMES) to each other is uncertain. NMES is widely applied in physiotherapy. In the SIS, the lower trapezius and serratus anterior muscle are affected. Therefore, our aim is to determine the effects of exercises and NMES used in patients with SIS on pain, range of motion (ROM), muscle strength and functional status, neck pain and sleep quality.

NCT ID: NCT04633083 Completed - Clinical trials for Shoulder Impingement

Range-of-motion Analysis of Reverse Shoulder Arthroplasty

ROM
Start date: March 20, 2019
Phase: N/A
Study type: Interventional

Limited range-of-motion (ROM) is a common problem after reverse shoulder arthroplasty (RSA). The occurrence and magnitude depend on both surgical and patient-related factors. The most important surgical factor is the occurrence of impingement, which implicates collision between the humeral implant or bone and the scapula, limiting further motion. Patient-related factors such as scapula geometry and muscle function and activation also play an important role. Surgeons have to account for these factors when planning and implanting a RSA. Software models can support the surgeon during preoperative planning by using imaging data to simulate the ROM of a patient's shoulder after RSA. These software models allow for adaptation of the implant position during preoperative planning and, by this optimize the postoperative ROM. However, the models currently developed are limited in terms of ROM simulation and the factors the models take into account.